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dc.contributor.author Katona, Gábor
dc.contributor.author Sultesz M
dc.contributor.author Farkas Z
dc.contributor.author Gyimesi A
dc.contributor.author Hirschberg A
dc.contributor.author Huszka J
dc.contributor.author Radvanszky F
dc.contributor.author Simon A
dc.contributor.author Fulop G
dc.contributor.author Lang J
dc.contributor.author Ablonczy, Mária
dc.contributor.author Nirnberger G
dc.contributor.author Holm C
dc.date.accessioned 2016-07-20T11:07:07Z
dc.date.available 2016-07-20T11:07:07Z
dc.date.issued 2015
dc.identifier.citation pagination=38, 8 p; journalVolume=5; journalTitle=CLINICAL AND TRANSLATIONAL ALLERGY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2644
dc.identifier.uri doi:10.1186/s13601-015-0084-5
dc.description.abstract BACKGROUND: In this observational trial, data were collected on the effectiveness and tolerability/safety of a nasal spray containing tramazoline and essential oils (trade name Rhinospray((R)) Plus) used for symptomatic treatment of acute rhinitis due to common cold. METHODS: The trial was performed in 300 children, adolescents and adults, who were to be treated with Rhinospray((R)) Plus for up to 4 times per day for up to 10 days. Primary endpoints were the change from baseline to final visit in the mean of three single symptom scores (blocked nose, sneezing, and runny nose) and the mean improvement in two quality-of-life parameters (ability to perform normal daytime activities and quality of sleep). RESULTS: A total of 108 children, 30 adolescents and 162 adults were treated with Rhinospray((R)) Plus. No patient discontinued prematurely. There was a mean reduction of 2.0 +/- 0.6 (standard deviation) in nasal symptom scores from baseline to final visit; 297 of 300 of patients (99.0 %) reported an improvement. The mean value for improvement in quality-of-life parameters was 1.3 +/- 0.5. Improvement in daytime activities was reported by all 300 patients (100.0 %) and in quality of sleep by 292 patients (97.4 %). Effectiveness and tolerability were rated as 'very good' or 'good' by 95.4 % and 97.4 % of patients, respectively; the investigators rated effectiveness and tolerability as 'very good' or 'good' for 97.4 % and 100.0 % of patients, respectively. No adverse events were reported. CONCLUSIONS: Community-based patients reported a relief in acute rhinitis symptoms and improvement in quality of life as a result of treatment with Rhinospray((R)) Plus. Treatment was well-tolerated.
dc.relation.ispartof urn:issn:2045-7022
dc.title Treatment of acute rhinitis with a nasal spray containing tramazoline and essential oils: a multicenter, uncontrolled, observational trial
dc.type Journal Article
dc.date.updated 2015-11-24T11:38:20Z
dc.language.rfc3066 en
dc.identifier.mtmt 2974849
dc.identifier.pubmed 26539289
dc.mtmt.swordnote PMC PMC4632331


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